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1678 TIMM8A

1678

TIMM8A

translocase of inner mitochondrial membrane 8A

protein-coding

Homo sapiens

基因描述

Type Description
Definition translocase of inner mitochondrial membrane 8A

研究结论

Date Results Publications
2020-04-11 10:55:00 The authors show that human Tim8a is required for the assembly of Complex IV in neurons, which is mediated through a transient interaction with Complex IV assembly factors, in particular the copper chaperone COX17. 31682224
2014-02-01 10:08:00 The results of this study demonistrated that the syndrome of deafness-dystonia is cause by mutation of Timm8a. 23418071
2012-04-28 10:59:00 knockdown of the TIMM8A gene by RNA interference did not show an influence on the oxygen respiration rate and the mitochondrial membrane potentia 21984432
2010-09-15 22:06:00 Observational study of gene-disease association. (HuGE Navigator) 19913121
2010-09-15 22:06:00 Observational study of gene-disease association, gene-environment interaction, and pharmacogenomic / toxicogenomic. (HuGE Navigator) 20628086

名称对应

Type IDs
Synonymous DDP, DDP1, DFN1, MTS, TIM8
Gene
UniProtKB-ID: TIM8A_HUMAN, A0A2R8YDA8_HUMAN
UniprotKB: O60220, A0A2R8YDA8
UniParc: UPI000012D5E9, UPI000057A417
EMBL: BC006994, AL035422, BC015093, U66035, CH471115, AK312117, BC070284
Ensembl: ENSG00000126953
KO: hsa:1678
Nucleutide sequences
EMBL-CDS: AAH70284.1, AAH15093.1, EAX02854.1, AAH06994.1, AAC15946.1, BAG35053.1
Ensembl_TRS: ENST00000372902, ENST00000644112, ENST00000645279
Protein sequencees
Ensembl_PRO: ENSP00000361993, ENSP00000494239, ENSP00000494385
RefSeq: NP_001139423.1, NP_004076.1
Others
UniRef100: UniRef100_A0A2R8YDA8, UniRef100_O60220
UniRef90: UniRef90_A0A2R8YDA8, UniRef90_O60220
UniRef50: UniRef50_O60220, UniRef50_A0A2R8YDA8
UniGene: Hs.447877
CCDS: CCDS14481.1

全选

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